FDA 510(k) Applications Submitted by CLINICAL DATA, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K052591 |
09/21/2005 |
NANOPIA WIDE RANGE C-REACTIVE PROTEIN (CRP) REAGENT KIT |
CLINICAL DATA, INC. |
K040467 |
02/24/2004 |
VITALAB URIC ACID REAGENT |
CLINICAL DATA, INC. |
K040508 |
02/27/2004 |
VITALAB MAGNESIUM REAGENT |
CLINICAL DATA, INC. |
K040534 |
03/02/2004 |
VITALAB AMYLASE REAGENT |
CLINICAL DATA, INC. |
K040631 |
03/10/2004 |
VITALAB DIRECT BILIRUBIN REAGENT |
CLINICAL DATA, INC. |
K031042 |
04/01/2003 |
ATAC HEMOGLOBIN A1C REAGENT KIT |
CLINICAL DATA, INC. |
K031044 |
04/01/2003 |
ATAC PAK URIC ACID REAGENT AND ATAC CALIBRATOR |
CLINICAL DATA, INC. |
K071706 |
06/21/2007 |
ENVOY 500 HDL; CHOLESTEROL REAGENT KIT (MODEL# 55301), CALIBRATOR KIT (MODEL# 55118) |
CLINICAL DATA, INC. |
K033983 |
12/23/2003 |
VITALAB IRON REAGENT |
CLINICAL DATA, INC. |
K034000 |
12/24/2003 |
VITALAB TRIGLYCERIDES REAGENT AND VITALAB CALIBRATOR |
CLINICAL DATA, INC. |
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